My family and I are doing the Kiltwalk this year to raise money for Muscular Dystrophy UK, this charity is close to my heart as my little cousin, Holly suffers with FSHD, She is only 9. FSHD is a rare genetic muscle wasting disease that affects the muscles of your face, shoulders arms and legs making every day tasks more difficult. There is no cure for FSHD. Muscular Dystrophy UK provides support to people living with muscle wasting conditions, by funding groundbreaking research, providing support, advocating and helping people with Muscular Dystrophy get access to treatments. You can make a massive difference in people like Holly’s lives by donating. Any donations are greatly appreciated ❤️

Muscular Dystrophy UK is the charity for 111,000 people living with muscle-wasting conditions. They are making a difference today, providing vital information and support to help people live as independently as possible. They are making a difference for tomorrow, accelerating progress in research and driving the campaign for access to emerging treatments.